26 research outputs found

    Fano symmetric varieties with low rank

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    The symmetric projective varieties of rank one are all smooth and Fano by a classic result of Akhiezer. We classify the locally factorial (respectively smooth) projective symmetric GG-varieties of rank 2 which are Fano. When GG is semisimple we classify also the locally factorial (respectively smooth) projective symmetric GG-varieties of rank 2 which are only quasi-Fano. Moreover, we classify the Fano symmetric GG-varieties of rank 3 obtainable from a wonderful variety by a sequence of blow-ups along GG-stable varieties. Finally, we classify the Fano symmetric varieties of arbitrary rank which are obtainable from a wonderful variety by a sequence of blow-ups along closed orbits.Comment: 31 page

    Normality and smoothness of simple linear group compactifications

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    If G is a complex semisimple algebraic group, we characterize the normality and the smoothness of its simple linear compactifications, namely those equivariant GxG-compactifications which possess a unique closed orbit and which arise in a projective space of the shape P(End(V)), where V is finite dimensional rational G-module. Both the characterizations are purely combinatorial and are expressed in terms of the highest weights of V. In particular, we show that Sp(2r) (with r > 0) is the unique non-adjoint simple group which admits a simple smooth compactification.Comment: v2: minor changes, final version. To appear in Math.

    Screening, isolation, and characterization of glycosyl-hydrolase-producing fungi from desert halophyte plants

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    Fungal strains naturally occurring on the wood and leaves of the salt-excreting desert tree Tamarix were isolated and characterized for their ability to produce cellulose- and starch- degrading enzymes. Of the 100 isolates, six fungal species were identified by ITS1 sequence analysis. No significant differences were observed among taxa isolated from wood samples of different Tamarix species, while highly salt-tolerant forms related to the genus Scopulariopsis (an anamorphic ascomycete) occurred only on the phylloplane of T. aphylla. All strains had cellulase and amylase activities, but the production of these enzymes was highest in strain D, a Schizophyllum-commune- related form. This strain, when grown on pretreated Tamarix biomass, produced an enzymatic complex containing levels of filter paperase (414 ± 16 IU/ml) that were higher than those of other S. commune strains. The enzyme complex was used to hydrolyze different lignocellulosic substrates, resulting in a saccharification rate of pretreated milk thistle (73.5 ± 1.2 %) that was only 10 % lower than that obtained with commercial cellulases. Our results support the use of Tamarix biomass as a useful source of cellulolytic and amylolytic fungi and as a good feedstock for the economical production of commercially relevant cellulases and amylases. [Int Microbiol 2014; 17(1):41-48]Keywords: Schizophyllum commune · Tamarix ssp. · cellulase activity · amylase activit

    SMOOTH PROJECTIVE SYMMETRIC VARIETIES WITH PICARD NUMBER ONE

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    GazeNeRF: 3D-Aware Gaze Redirection with Neural Radiance Fields

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    We propose GazeNeRF, a 3D-aware method for the task of gaze redirection. Existing gaze redirection methods operate on 2D images and struggle to generate 3D consistent results. Instead, we build on the intuition that the face region and eyeballs are separate 3D structures that move in a coordinated yet independent fashion. Our method leverages recent advancements in conditional image-based neural radiance fields and proposes a two-stream architecture that predicts volumetric features for the face and eye regions separately. Rigidly transforming the eye features via a 3D rotation matrix provides fine-grained control over the desired gaze angle. The final, redirected image is then attained via differentiable volume compositing. Our experiments show that this architecture outperforms naively conditioned NeRF baselines as well as previous state-of-the-art 2D gaze redirection methods in terms of redirection accuracy and identity preservation

    Bone sarcoma patient-derived xenografts are faithful and stable preclinical models for molecular and therapeutic investigations

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    Standard therapy of osteosarcoma (OS) and Ewing sarcoma (EW) rests on cytotoxic regimes, which are largely unsuccessful in advanced patients. Preclinical models are needed to break this impasse. A panel of patient-derived xenografts (PDX) was established by implantation of fresh, surgically resected osteosarcoma (OS) and Ewing sarcoma (EW) in NSG mice. Engraftment was obtained in 22 of 61 OS (36%) and 7 of 29 EW (24%). The success rate in establishing primary cell cultures from OS was lower than the percentage of PDX engraftment in mice, whereas the reverse was observed for EW; the implementation of both in vivo and in vitro seeding increased the proportion of patients yielding at least one workable model. The establishment of in vitro cultures from PDX was highly efficient in both tumor types, reaching 100% for EW. Morphological and immunohistochemical (SATB2, P-glycoprotein 1, CD99, caveolin 1) studies and gene expression profiling showed a remarkable similarity between patient's tumor and PDX, which was maintained over several passages in mice, whereas cell cultures displayed a lower correlation with human samples. Genes differentially expressed between OS original tumor and PDX mostly belonged to leuykocyte-specific pathways, as human infiltrate is gradually replaced by murine leukocytes during growth in mice. In EW, which contained scant infiltrates, no gene was differentially expressed between the original tumor and the PDX. A novel therapeutic combination of anti-CD99 diabody C7 and irinotecan was tested against two EW PDX; both drugs inhibited PDX growth, the addition of anti-CD99 was beneficial when chemotherapy alone was less effective. The panel of OS and EW PDX faithfully mirrored morphologic and genetic features of bone sarcomas, representing reliable models to test therapeutic approaches

    Effective and big divisors on a projective symmetric variety

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    Je décris les cônes effectif et gros d'une variété symétrique projective. De plus, je donne un critère combinatoire nécessaire et suffisant combinatoire afin que un diviseur nef sur une variété symétrique projective soit gros. Quand le diviseur est la G-stable, un tel critère a une interprétation géométrique explicite. Finalement, je décris la clôture sphérique d'un sous-groupe symétrique
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